Three-dimensional (3D) printing is an attractive technology in dentistry. Acrylic-based 3D printed resin parts have to undergo postcuring processes to enhance their mechanical and biological properties, such as UV-light and thermal polymerization. However, no previous studies have revealed how the postcuring temperature influences the biocompatibility of the produced parts. Therefore, we postprocessed 3D printed denture teeth resin under different postcuring temperatures (40, 60 and 80 °C) for different periods (15, 30, 60, 90 and 120 min), and evaluated their flexural properties, Vickers hardness, cell cytotoxicity, cell viability, and protein adsorption. In addition, confocal laser scanning was used to assess the condition of human gingival fibroblasts. It was found that increasing the postcuring temperature significantly improved the flexural strength and cell viability. The flexural strength and cell viability were 147.48 ± 5.82 MPa (mean ± standard deviation) and 89.51 ± 7.09%, respectively, in the group cured at 80 °C for 120 min, which were higher than the values in the 40 and 60 °C groups. The cell cytotoxicity increased in the 40 °C groups and for longer cultivation time. Confocal laser scanning revealed identifiable differences in the morphology of fibroblasts. This study has confirmed that the postcuring temperature influences the final mechanical and biological properties of 3D printed resin.

Despite the substantial contribution of titanium implants in the field of dental and orthopedic reconstructive therapy, there is a crucial unaddressed question of why bone-implant contact does not reach the ideal 100%. This review article introduces the recently reported time-dependent reduction in osteoconductivity and other biological capabilities of titanium since processing. This phenomenon is defined as the biological aging of titanium and provides insight to significantly advance the understanding of osseointegration and to further improve implant surfaces in the future.

Here, we evaluated time-dependent changes in the effects of ultraviolet (UV) and nonthermal atmospheric pressure plasma (NTAPPJ) on the biological activity of titanium compared with that of untreated titanium. Grade IV machined surface titanium discs (12-mm diameter) were used immediately and stored up to 28 days after 15-min UV or 10-min NTAPPJ treatment. Changes of surface characteristics over time were evaluated using scanning electron microscopy, surface profiling, contact angle analysis, X-ray photoelectron spectroscopy, and surface zeta-potential. Changes in biological activity over time were as determined by analysing bovine serum albumin adsorption, MC3T3-E1 early adhesion and morphometry, and alkaline phosphatase (ALP) activity between groups. We found no differences in the effects of treatment on titanium between UV or NTAPPJ over time; both treatments resulted in changes from negatively charged hydrophobic (bioinert) to positively charged hydrophilic (bioactive) surfaces, allowing enhancement of albumin adsorption, osteoblastic cell attachment, and cytoskeleton development. Although this effect may not be prolonged for promotion of cell adhesion until 4 weeks, the effects were sufficient to maintain ALP activity after 7 days of incubation. This positive effect of UV and NTAPPJ treatment can enhance the biological activity of titanium over time.

Objective: Ultraviolet (UV) light treatment of titanium, ie, photofunctionalization, has been extensively reported to enhance the osteoconductivity of titanium in animal and in vitro studies. This is the first study to examine whether photofunctionalization is effective on commercial dental implants in vivo. Materials and Methods: Dental implants with a microroughened surface were placed into dog jawbones. Photofunctionalization was performed by treating implants with UV light for 15 minutes using a photo device immediately before placement. Four weeks after placement, bone-implant integration was evaluated using a removable torque test and static and dynamic histology. Results: Implant surfaces were converted from hydrophobic to super-hydrophilic after photofunctionalization. Removable torque for photofunctionalized implants was significantly higher by 50% than that for untreated implants. Bone-implant contact (BIC) was significantly higher for photofunctionalized implants in all zones examined: marginal, cortical, and bone marrow zones. An intensive mineralized layer was exclusively present in marginal bone at photofunctionalized interface. Dynamic histology identified early-onset, long-lasting robust bone deposition at photofunctionalized interface. Conclusions: Photofunctionalization enhanced the morphology, quality, and behavior of periimplant osteogenesis, including the increased BIC, expedited robust interfacial bone deposition, and improved marginal bone seal and support.